Detailed mechanisms of signal transduction pathways of AngII in chromaffin cells
Detailed mechanisms of signal transduction pathways of AngII in chromaffin cells
批准号:
15590967
负责人:
TAKEKOSHI Kazuhiro
金额:
$2.18万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2003
资助国家:
日本
项目状态:
已结题
起止时间:
2003 至 2005
中文摘要
血管紧张素II受体AT_1和AT_2是两种截然不同的受体。我们先前已经证明,刺激AT_2会降低培养的猪嗜铬细胞内cGMP水平,其中AT_2是主要表达的受体。然而,AT_1或AT_2是否影响嗜铬细胞的信号转导通路尚不清楚。利用基因芯片技术,比较了AngiI+CV-11974(模拟AT_2刺激的AT1拮抗剂)和AngiI+PD 123319(模拟AT_1刺激的AT_2拮抗剂)的作用。在这种情况下,有几个基因表达下调和过度表达。我们正在描述这些基因的特征。
英文摘要
Two distinct types of angiotensin II (AngII) receptors, AT_1 and AT_2, have been cloned. We have previously shown that stimulation of AT_2 reduces intracellular cGMP levels in cultured porcine chromaffin cells in which AT_2 is the predominantly expressed receptor. However, it has not been determined whether AT_1 or AT_2 affects signal transduction pathways in chromaffin cells. Using Genetic Micro System(GMS-418-array scanner), we compare the effects of AngII plus CV-11974 (an AT_1 antagonist, which simulates specific AT_2 stimulation) with AngII plus PD 123319 (an AT_2 antagonist, which simulates specific AT_1 stimulation). There are several genes down and over expressed under such condition. We are characterize these genes.
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Inhibition of the RhoA/Rho kinase system attenuates catecholamine biosynthesis in PC12 celles
抑制 RhoA/Rho 激酶系统会减弱 PC12 细胞中儿茶酚胺的生物合成
DOI:
--
发表时间:
2005
期刊:
Biochemica et Biophysica Acta 1726(1)
影响因子:
--
作者:
[Fukuda T, Takekoshi K, et al.]
通讯作者:
et al.
Urocortin stimulates tyrosine hydroxylase activity via the cAMP/protein kinase pathway in rat Pheochromocytoma PC12 cells.
Urocortin 通过 cAMP/蛋白激酶途径刺激大鼠嗜铬细胞瘤 PC12 细胞中的酪氨酸羟化酶活性。
DOI:
--
发表时间:
2005
期刊:
Neuroscience Letters 382(1-2)
影响因子:
--
作者:
[Nanmoku T, Takekoshi K, Fukuda T, Isobe K, Shibuya S, Kawakami Y.]
通讯作者:
Kawakami Y.
Vrocortin stimulates tyrosine hydroxylue activiy via the cAMP/PKA pathway in PC 12 cells
Vrocortin 通过 PC 12 细胞中的 cAMP/PKA 途径刺激酪氨酸羟基活性
DOI:
--
发表时间:
2005
期刊:
Neuroscience Letters 382(1-2)
影响因子:
--
作者:
[Nanmoku T, Takekoshi K, et al.]
通讯作者:
et al.
Stimulation of catecholamine biosynthesis via the PKC pathway by prolactin-releasing peptide in PC12 rat pheochromocytoma cells.
PC12 大鼠嗜铬细胞瘤细胞中催乳素释放肽通过 PKC 途径刺激儿茶酚胺生物合成。
DOI:
--
发表时间:
2005
期刊:
J Endocrinol. 186(1)
影响因子:
--
作者:
[Yatoh S, Mizutani M, Yokoo T, Kozawa T, Sone H, Toyoshima H, Suzuki S, Shimano H, Kawakami Y, Okuda Y, Yamada N., 川上 康, 川上 康]
通讯作者:
川上 康
Stimulation of catecholamine biosynthesis via PKC pathway prolactin-releasing peptide in 12 cells
通过 PKC 途径催乳素释放肽在 12 个细胞中刺激儿茶酚胺生物合成
DOI:
--
发表时间:
2005
期刊:
Journal of Endocrinology 186(1)
影响因子:
--
作者:
[Nanmoku T, Takekoshi K, et al.]
通讯作者:
et al.
共 7 条
Renalase in the skeletal muscle contributes to cell protective effect
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批准号:17K01839
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.16万
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财政年份:2017
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负责人:TAKEKOSHI Kazuhiro
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依托单位:
A Common Genetic Variant of the Chromogranin A-derived peptide Catestatin is Associated with Atherogenesis and Hypertension in a Japanese Population
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批准号:26350881
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.16万
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财政年份:2014
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负责人:TAKEKOSHI Kazuhiro
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依托单位:
Research of SDHB as Malignant marker and oncogenesis in malignant pheochromocytomas
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批准号:21591168
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.0万
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财政年份:2009
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负责人:TAKEKOSHI Kazuhiro
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依托单位: